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Introduction

This webinar will evaluate medical device review routes under Exempt, 510(k) / PMN, and PMA, as both a process and as documentation / submissions. The 510(k) process and submission documentation, the role of the IDE, and the PMA process and submission documentation will be evaluated and discussed.

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Venue

Online Training

Livermore Common, Online Training, California, Fremont, 94539, United States

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Organised by

GlobalCompliancePanel

Contact information

Mr John Robinson
Livermore Common, Fremont, 94539, United States of America
8004479407
Contact us by email

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